Opera Mariposa 2023 Benefit & Awareness Month

I’m so excited to be taking part in Opera Mariposa’s 2023 Benefit + Awareness Month🦋 I’m joining them as a featured artist in their online art showcase, as well as having some of my artwork appearing in their charity prize draw!

Against a gauzy blue background, Jacqueline Ko spins in a sea blue chiffon gown, her long black hair flowing, haloed in rays of light. Next to logos of Opera Mariposa and the ME FM Society of BC, white text reads, Opera Mariposa's 2023 Benefit + Awareness Month. May 1 - June 1. Benefit.OperaMariposa.com.

This entire charity fundraiser runs May 1-June 1 at Benefit.OperaMariposa.com, and features music, videos, art, merchandise, nearly $5,000 in prizes and more! It’s all in support of the ME/FM Society of BC and the rising number of people impacted by Myalgic Encephalomyelitis (ME), Fibromyalgia (FM) and Long Covid. There are free and by-donation ways to take part—plus, donations will be TRIPLED up to $3,500, so your support has three times the impact! I hope you’ll check it out, and join me in support of the chronic illness community.

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The Body Electric 2021 & 2022

My work was once again selected to appear in The Body Electric—an annual health and humanities exhibit that is part of the International Conference on Residency Education (ICRE).

Initially launched during the 2014 International Conference, The Body Electric uses art as a way to critically engage with medicine and healthcare. The Body Electric annual digital art exhibit showcases an inspiring selection of visual art, in a range of media, including photography, drawing, painting, sculpture and video.  

from The Body Electric website

One of this year’s themes was Art as Coping so I submitted three of my paresthesia symptomatology pieces:

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Visible Mending

Since taking up hand stitching again in 2016, I discovered I needed something simpler to work on in the evenings and on weekends than my very intricate embroidery pieces. I discovered Visible Mending through some embroiderers on Instagram and it’s become an excellent hobby.

The butt of a pair of black jeans with a Japanese wave pattern on them done in grey sashiko stitching.

I started with some simple sashiko mends on my son’s jeans which got more intricate the more I learned about sashiko techniques. Susan Briscoe’s excellent book—The Ultimate Sashiko Sourcebook—has been a great resource for this.

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Upcoming Anthology Publication: In Corpore Sano

I have reached a point in my recovery from ME/CFS that means I am able to write again! ME/CFS is a neuro-immune disease and some of the symptoms include brain fog and cognitive fatigue. When I first got ill in 2015 I was unable to read or write for any length of time because it would utterly exhaust me. I’m very happy to say that I can now read and write with relative ease again.

Most of my writing these days is in the form of journaling, but earlier this year I submitted some of my embroidery work to an anthology about “challenged bodies” and creative work. As part of the In Corpore Sano anthology I was asked to write about my experience of being a creative person living with a debilitating illness and wrote a fairly long essay about that as well as the autobiographical and therapeutic nature of my embroidery work.  Continue reading

Featured Artist in Synaesthesia Magazine

I was recently featured in Synaesthesia magazine as their artist of the month. The piece focuses on the embroidery work I’ve done to illustrate my ME/CFS symptoms.

I was also the rocur (rotating curator) of @IAmSciArt on Twitter for a week in November and you can see more of my embroidery here (though these links will only work until May 2018). There are two threads, one on anatomy-themed embroideries, and the other on my symptomatology embroideries.

I’m currently working on a large anatomy-themed piece that you can check the progress on my Instagram.

Healthwise, I’m very slowly improving after a bit of a downturn in the fall because of a stomach flu. I’m still mostly housebound but have been able to drive myself to a few appointments and attend a few family gatherings. If you want to know more about ME/CFS I recommend watching the documentary Unrest, which is on iTunes and Netflix.